open access publication

Article, 2024

Impaired skeletal muscle regeneration in diabetes: From cellular and molecular mechanisms to novel treatments

Cell Metabolism, ISSN 1550-4131, 1932-7420, Volume 36, 6, Pages 1204-1236, 10.1016/j.cmet.2024.02.014

Contributors

Espino-Gonzalez, Ever 0000-0001-5371-227X [1] Dalbram, Emilie 0000-0002-7679-5896 [1] Mounier, RĂ©mi [2] Gondin, Julien [2] Farup, Jean Gammelgaard 0000-0002-7579-6512 [3] [4] Jessen, Niels 0000-0001-5613-7274 [3] [4] Treebak, Jonas Thue 0000-0003-1488-7012 (Corresponding author) [1]

Affiliations

  1. [1] University of Copenhagen
  2. [NORA names: KU University of Copenhagen; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] University of Lyon System
  4. [NORA names: France; Europe, EU; OECD];
  5. [3] Aarhus University
  6. [NORA names: AU Aarhus University; University; Denmark; Europe, EU; Nordic; OECD];
  7. [4] Aarhus University Hospital
  8. [NORA names: Central Denmark Region; Hospital; Denmark; Europe, EU; Nordic; OECD]

Abstract

Diabetes represents a major public health concern with a considerable impact on human life and healthcare expenditures. It is now well established that diabetes is characterized by a severe skeletal muscle pathology that limits functional capacity and quality of life. Increasing evidence indicates that diabetes is also one of the most prevalent disorders characterized by impaired skeletal muscle regeneration, yet underlying mechanisms and therapeutic treatments remain poorly established. In this review, we describe the cellular and molecular alterations currently known to occur during skeletal muscle regeneration in people with diabetes and animal models of diabetes, including its associated comorbidities, e.g., obesity, hyperinsulinemia, and insulin resistance. We describe the role of myogenic and non-myogenic cell types on muscle regeneration in conditions with or without diabetes. Therapies for skeletal muscle regeneration and gaps in our knowledge are also discussed, while proposing future directions for the field.

Keywords

alterations, animal models, animal models of diabetes, animals, capacity, cell types, comorbidities, concerns, conditions, diabetes, direction, disorders, evidence, expenditure, field, functional capacity, gap, health concern, healthcare, healthcare expenditures, human life, impact, impaired skeletal muscle regeneration, knowledge, life, limited functional capacity, mechanism, models of diabetes, molecular alterations, muscle, muscle pathology, muscle regeneration, non-myogenic cell types, novel treatment, pathology, people, prevalent disorders, public health concern, quality, quality of life, regeneration, review, skeletal muscle pathology, skeletal muscle regeneration, therapeutic treatment, therapy, treatment, type

Funders

  • Novo Nordisk Foundation

Data Provider: Digital Science